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Glycogen Synthase Kinase 3β Inhibitor (2'Z,3'E)-6-Bromo-indirubin- 3'-Oxime Enhances Drug Resistance to 5-Fluorouracil Chemotherapy in Colon Cancer Cells.pdfVIP

Glycogen Synthase Kinase 3β Inhibitor (2'Z,3'E)-6-Bromo-indirubin- 3'-Oxime Enhances Drug Resistance to 5-Fluorouracil Chemotherapy in Colon Cancer Cells.pdf

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Glycogen Synthase Kinase 3β Inhibitor (2'Z,3'E)-6-Bromo-indirubin- 3'-Oxime Enhances Drug Resistance to 5-Fluorouracil Chemotherapy in Colon Cancer Cells.pdf

工6 ChinjCancerRes24(2):116-123,2012 www.springerlink.cam 谳 GlycogenSynthaseKinase3pInhibitor(2Z,3’E)一6一Bromo—indirubin- 3-OximeEnhancesDrugResistanceto5-Fluorouracil ChemotherapyinColonCancerCells Kun—pingLiu,, FengLuo , Si-mingXie。 , Li-juanTang, Mei—xiangthen, Xue—fangWu, Xue—yunZhong TongZhaoJ DepartmentofPathology,NanfangHospital,SouthernMedicalUniversity,Guangzhou51051~China DepartmentofPathology,QingyuanHospital,MedicalCollege,JinanUniversity,Qingyuan51151China DepartmentofPathology,MedicalCollege,JinanUniversity,Guangzhou51063ZChina Departmento/Pathology,SchoolofBasicMedicalScience,SouthernMedicalUniversity,Guangzhou51051~China DOI:10.1007/s11670-012—0116·9 ~ChineseAnti-CancerAssociationandSpringer-VerlagBerlinHeidelberg2012 ABSTRACr 0bjective:To explore the effects and mechanism ofglycogen synthase kinase 313 (GSK一3B) inhibitor (2。Z,3’E)一6一bromo—indirubin一3-oxime(BIO)ondrugresistanceincoloncancercells. Methods:ThecoloncancerSW480andSW620cellsweretreatedwithBIO,5一fluorouraciI(5一Fu)andBIO/S—FU, separately.CelIcycledistribution,apoptosislevelande仟luxabilityofrhodamine123(Rh123)weredetectedbyflow cytometry.Theproteinexpressionsofp--glycoprotein(p-gP),multidrugresistanceprotein2(MRP2),thymidylatesynthase (Ts),13一catenin,E2F一1and Bcl-2were detectedbyWestern blot.B—cateninand p-.gPwere stainedwith double immunofluorescenceandobservedunderaconfocalmicroscope. Results:BIOup—regulated3-catenin,p-gP,MRP2andTS,enhancedthee仟luxabilityofRh123,decreasedBcl~2protein andgavetheoppositee仟ectto E2F一1proteininSW480andSW620cells.Fu~hermore,B10 significantly inhibitedcelI apoptosis,increasedSandG2/Mphasecells,andreducedthecelIapoptosisinducedby5一FUinSW480cells,whereasthe effectswereslightornotobviousinSW620cells. Con

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